Amino-, Alkoxy-, and Alkylthio-Isocyanates and – Isothiocyanates, RX-NCY, their Isomers RX-YCN and RX-CNY, and their Rearrangements

Curt      Wentrup; Justin      J. Finnerty; Rainer      Koch

doi:10.2174/138527211795656624

Abstract

Hetero-substituted isocyanates and isothiocyanates RX-NCY (X = R2N, RO, or RS; Y = O or S) and the isomeric cyanates RX-OCN, thiocyanates RX-SCN, nitrile oxides RX-CNO, and nitrile sulfides RX-CNS are highly reactive compounds, often transient at room temperature. The chemistry of these compounds is reviewed. A number of rearrangement reactions is described, particularly [3,3]- sigmatropic shifts, e.g. PhX-NCY → o-HX-C6H4-YCN (X = NR, O, S; Y = O, S); and retro-ene type reactions, RCH2X-NCY → RCH=X + HYCN (X = NR, O, S; Y = O, S). In addition, potential 1,4-shifts of substituent groups of the type R-Y-CNX → R-X-N=C=Y; 1,3- shifts R-C(=Y)-N=X → R-X-N=C=Y; and 1,2-shifts R-C(=Y)-N=X → R-Y-CNX were identified computationally.

Keywords: Isocyanates, isothiocyanates, cyanates, thiocyanates, nitrile oxides, nitrile sulfides, acylisothiocyanates/thioacylisocyanates, AMINOISOTHIOCYANATES, REARRANGEMENTS, thiophosgene, thiosemicarbazone, NCS bending, symmetric NCS stretching, analytical technique, ALKOXY ISOCYANATES